Variant report

Variant rs12000929
Chromosome Location chr9:16189225-16189226
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16179800-16192000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr9:16185200-16193600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:16185600-16192200 Weak transcription Primary T killer naive cells fromperipheralblood blood
4 chr9:16185600-16196400 Weak transcription Aorta Aorta
5 chr9:16187800-16191400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr9:16189000-16190000 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:16189200-16189800 ZNF genes & repeats Primary T cells from cord blood blood

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